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Triple mutations in three major genes for long QT syndrome are very rare and cause complicated phenotypes with ventricular arrhythmia

Session: Poster session 4 - Miscellaneous in arrhythmia
Topic: Genetic aspects of arrhythmias
Speaker: Doctor S. Ohno (Suita, JP)
Event: ESC Congress 2016

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Doctor Seiko Ohno

National Cerebral & Cardiovascular Center, Suita (Japan)
2 presentations
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28 more presentations in this session

A novel CACNA1C mutation identified in a patient with atypical Timothy syndrome exerts both loss- and gain-of-function effects on Cav1.2.

Speaker: Doctor J. Ozawa (Niigata, JP)

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Genetic testing in a consecutive series of young athletes with suspected cathecolaminargic polymorphic ventricular tachycardia

Speaker: Associate Professor N. Marziliano (Milan, IT)

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The burden of complex arrhythmic genotypes in a consecutive series of Sardinian population of patients with primary arrhythmic disorders

Speaker: Associate Professor N. Marziliano (Milan, IT)

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Discrepancy of QTc duration and LQTS risk score for the diagnosis of type 3 LQTS

Speaker: Doctor A. Hermida (Paris, FR)

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Complex inherited cardiac diseases inheritance in a family harbouring compound SCN5A and MYBPC3 mutations.

Speaker: Doctor R. Mango (Rome, IT)

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Poster session 4 - Miscellaneous in arrhythmia

Speakers: Doctor S. Ohno, Doctor J. Ozawa, Associate Professor N. Marziliano, Associate Professor N. Marziliano, Doctor A. Hermida...
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ESC Congress 2016

27 August - 31 August 2016

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